Transition Metal-Catalyzed C-H Amination: Scope, Mechanism, and Applications

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dc.contributor.authorPARK, YOONSUko
dc.contributor.authorKim, Youyoungko
dc.contributor.authorChang, Sukbokko
dc.date.accessioned2017-08-16T08:53:05Z-
dc.date.available2017-08-16T08:53:05Z-
dc.date.created2017-08-14-
dc.date.created2017-08-14-
dc.date.created2017-08-14-
dc.date.created2017-08-14-
dc.date.issued2017-07-
dc.identifier.citationCHEMICAL REVIEWS, v.117, no.13, pp.9247 - 9301-
dc.identifier.issn0009-2665-
dc.identifier.urihttp://hdl.handle.net/10203/225332-
dc.description.abstractCatalytic transformation of ubiquitous C-H bonds into valuable C-N bonds offers an efficient synthetic approach to construct N-functionalized molecules. Over the last few decades, transition metal catalysis has been repeatedly proven to be a powerful tool for the direct conversion of cheap hydrocarbons to synthetically versatile amino-containing compounds. This Review comprehensively highlights recent advances in intra- and intermolecular C-H amination reactions utilizing late transition metal based catalysts. Initial discovery, mechanistic study, and additional applications were categorized on the basis of the mechanistic scaffolds and types of reactions. Reactivity and selectivity of novel systems are discussed in three sections, with each being defined by a proposed working mode.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleTransition Metal-Catalyzed C-H Amination: Scope, Mechanism, and Applications-
dc.typeArticle-
dc.identifier.wosid000405642800019-
dc.identifier.scopusid2-s2.0-85024117498-
dc.type.rimsART-
dc.citation.volume117-
dc.citation.issue13-
dc.citation.beginningpage9247-
dc.citation.endingpage9301-
dc.citation.publicationnameCHEMICAL REVIEWS-
dc.identifier.doi10.1021/acs.chemrev.6b00644-
dc.contributor.localauthorPARK, YOONSU-
dc.contributor.localauthorChang, Sukbok-
dc.description.isOpenAccessN-
dc.type.journalArticleReview-
dc.subject.keywordPlusN BOND-FORMATION-
dc.subject.keywordPlusCARBON-HYDROGEN BONDS-
dc.subject.keywordPlusVISIBLE-LIGHT PHOTOREDOX-
dc.subject.keywordPlusINTRAMOLECULAR C(SP(2))-H AMINATION-
dc.subject.keywordPlusNITROGEN-CONTAINING HETEROCYCLES-
dc.subject.keywordPlusUNACTIVATED C(SP(3))-H BONDS-
dc.subject.keywordPlusAEROBIC OXIDATIVE AMINATION-
dc.subject.keywordPlusNITRENE TRANSFER-REACTIONS-
dc.subject.keywordPlusBENZYLIC METHYLENE GROUPS-
dc.subject.keywordPlusO-BENZOYL-HYDROXYLAMINES-
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